Status:
COMPLETED
Effect of Buffered Numbing Solution on Patients With Toothaches
Lead Sponsor:
Ohio State University
Conditions:
Irreversible Pulpitis (Toothache)
Eligibility:
All Genders
18-65 years
Phase:
NA
Brief Summary
The purpose of this study is to determine the effect of buffered lidocaine (a numbing solution) on the ability to numb patients with toothaches. Buffered anesthetic (numbing) solutions have shown prom...
Eligibility Criteria
Inclusion
- patients with a diagnosis of irreversible pulpitis (toothache) in a mandibular posterior tooth (back/bottom tooth) with moderate to severe pain
- ages 18 -65 years of age
- in good health (ASA I or II)
- able to grant informed consent.
Exclusion
- allergy to lidocaine (numbing solution
- significant medical problem (ASA III or IV)
- have taken CNS depressants or analgesic medications within the last 24 hours
- pregnancy or lactating
- non-English speaking
- inability to give informed consent
Key Trial Info
Start Date :
March 1 2013
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2013
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT01868776
Start Date
March 1 2013
End Date
December 1 2013
Last Update
October 6 2020
Active Locations (1)
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1
The Ohio State University College of Dentistry, Postle Hall
Columbus, Ohio, United States, 43210